Synthesis and Biological Evaluation of Inhibitors of Topoisomerases and Histone Deacetylase for In Vitro Anticancer Activity
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Date
2019
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Central University of Punjab
Abstract
Topoisomerases (Topos) and histone deacetylases (HDACs) are validated oncotherapeutic targets due to their involvement in most of the cellular events such as initiation, proliferation, and survival of cancer cells. Widespread research has undergone to design and discover small molecule inhibitors of each protein which has led to the development of several drugs that are making their presence felt in clinic. Considering the issues of stability, toxicity, reported crosstalk(s) and resitance of existing pharmacophores, we herein report the discovery of target-based molecules pertaining to pyrazolo[1,5-c]quinazolines, 2-aryl quinolines and imidazo[1,2- a]quinoxaline scaffolds as inhibitors of TopoI or dual TopoI and II designed rationally via in silico tools. The chemical space of scaffolds was further exploited to design and synthesise dual/multi inhibitors of Topo-HDAC by connecting pharmacophoric features of HDAC inhibitors via a linker. Detailed biological evaluation of synthetics was performed using multiple cancer cell lines as well as normal cells/cell lines. Utilizing MTT, dye exclusion, redox potential, cell cycle and annexin V vs PI assays in 2D as well as 3D cultures, we established their preferential cytotoxic potential. Signaling responsible for anticancer mechanism was delineated using western immunoblotting and qPCR assays. Further, in vitro assays v for topoisomerases (DNA relaxation and catenation), and/or HDAC1 revealed target specificity of synthetics. In addition, we also demonstrated a novel bioreductive methodology, specific to cancer cells, exploiting cancer microenvironment leading to delivery of molecularly targeted agents as topo(s) inhibitors.
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Keywords
Cancer, Topoisomerases, Histone deacetylase
Citation
Joshi, Gaurav, Kumar, Raj & Singh, Sandeep (2019) Synthesis and Biological Evaluation of Inhibitors of Topoisomerases and Histone Deacetylase for In Vitro Anticancer Activity